Canonical Allele Identifier: PA2829603567
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1462026
ClinVar RCV Id: RCV001968252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Asp357Glu
CA342820316
NM_005572.4:c.1071C>A
CA342820317
NM_005572.4:c.1071C>G